@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP728480.RASDFS95XDWGQVUt9rkt8h5b0_P_9eyMM4NmZXRaUE89I
> .
@prefix rdfs: <
http://www.w3.org/2000/01/rdf-schema#
> .
@prefix xsd: <
http://www.w3.org/2001/XMLSchema#
> .
@prefix sio: <
http://semanticscience.org/resource/
> .
@prefix ncit: <
http://ncicb.nci.nih.gov/xml/owl/EVS/Thesaurus.owl#
> .
@prefix lld: <
http://linkedlifedata.com/resource/umls/id/
> .
@prefix miriam-gene: <
http://identifiers.org/ncbigene/
> .
@prefix miriam-pubmed: <
http://identifiers.org/pubmed/
> .
@prefix eco: <
http://purl.obolibrary.org/obo/eco.owl#
> .
@prefix wi: <
http://purl.org/ontology/wi/core#
> .
@prefix prov: <
http://www.w3.org/ns/prov#
> .
@prefix pav: <
http://purl.org/pav/2.0/
> .
@prefix prv: <
http://purl.org/net/provenance/ns#
> .
@prefix dcterms: <
http://purl.org/dc/terms/
> .
@prefix np: <
http://www.nanopub.org/nschema#
> .
@prefix dgn-np: <
http://rdf.disgenet.org/nanopublications.trig#
> .
@prefix dgn-gda: <
http://rdf.disgenet.org/gene-disease-association.ttl#
> .
@prefix dgn-void: <
http://rdf.disgenet.org/v2.1.0/void.ttl#
> .
dgn-np:NP728480.RASDFS95XDWGQVUt9rkt8h5b0_P_9eyMM4NmZXRaUE89I130_head
{
this:
np:hasAssertion
dgn-np:NP728480.RASDFS95XDWGQVUt9rkt8h5b0_P_9eyMM4NmZXRaUE89I130_assertion
;
np:hasProvenance
dgn-np:NP728480.RASDFS95XDWGQVUt9rkt8h5b0_P_9eyMM4NmZXRaUE89I130_provenance
;
np:hasPublicationInfo
dgn-np:NP728480.RASDFS95XDWGQVUt9rkt8h5b0_P_9eyMM4NmZXRaUE89I130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP728480.RASDFS95XDWGQVUt9rkt8h5b0_P_9eyMM4NmZXRaUE89I130_assertion
a
np:Assertion
.
dgn-np:NP728480.RASDFS95XDWGQVUt9rkt8h5b0_P_9eyMM4NmZXRaUE89I130_provenance
a
np:Provenance
.
dgn-np:NP728480.RASDFS95XDWGQVUt9rkt8h5b0_P_9eyMM4NmZXRaUE89I130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP728480.RASDFS95XDWGQVUt9rkt8h5b0_P_9eyMM4NmZXRaUE89I130_assertion
{
miriam-gene:6361
a
ncit:C16612
.
lld:C0004096
a
ncit:C7057
.
dgn-gda:DGN395eae0e555393b87311755692eb8ccc
sio:SIO_000628
miriam-gene:6361
,
lld:C0004096
;
a
sio:SIO_001121
.
}
dgn-np:NP728480.RASDFS95XDWGQVUt9rkt8h5b0_P_9eyMM4NmZXRaUE89I130_provenance
{
dgn-np:NP728480.RASDFS95XDWGQVUt9rkt8h5b0_P_9eyMM4NmZXRaUE89I130_assertion
dcterms:description
"[This study does not support the existence in human asthma of the full M2 phenotype described to date but points to upregulation of CCL17 in both patients with mild and those with moderate asthma, providing a further source for this ligand of CCR4(+) cells that contributes to airways inflammation.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en ;
wi:evidence
dgn-void:source_evidence_literature
;
sio:SIO_000772
miriam-pubmed:22981793
;
prov:wasDerivedFrom
dgn-void:befree-20140225
;
prov:wasGeneratedBy
eco:ECO_0000203
.
dgn-void:befree-20140225
pav:importedOn
"2014-02-25"^^
xsd:date
.
dgn-void:source_evidence_literature
a
eco:ECO_0000212
;
rdfs:comment
"Gene-disease associations inferred from text-mining the literature."@en ;
rdfs:label
"DisGeNET evidence - LITERATURE"@en .
}
dgn-np:NP728480.RASDFS95XDWGQVUt9rkt8h5b0_P_9eyMM4NmZXRaUE89I130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:39:22+02:00"^^
xsd:dateTime
;
dcterms:rights
<
http://opendatacommons.org/licenses/odbl/1.0/
> ;
dcterms:rightsHolder
dgn-void:IBIGroup
;
dcterms:subject
sio:SIO_000983
;
prv:usedData
dgn-void:disgenetrdf
;
pav:authoredBy
<
http://orcid.org/0000-0001-5999-6269
> , <
http://orcid.org/0000-0002-7534-7661
> , <
http://orcid.org/0000-0002-9383-528X
> , <
http://orcid.org/0000-0003-0169-8159
> , <
http://orcid.org/0000-0003-1244-7654
> ;
pav:createdBy
<
http://orcid.org/0000-0003-0169-8159
> ;
pav:version
"v2.1.0.0" .
dgn-void:disgenetrdf
pav:version
"v2.1.0" .
}